Makcin (Clarithromycin)

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Medically reviewed

Marina Burgos

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Makcin (Clarithromycin)

Property Description
Active ingredient Clarithromycin
Form Oral tablets (immediate and modified-release) and oral suspension
Pharmacological class Macrolide Antibiotic
Common use Systemic treatment of bacterial infections
Origin Semisynthetic (derived from Erythromycin)

What is Makcin (Clarithromycin) and What Type of Antibiotic Is It?

Makcin is a prescription-only medication containing the active ingredient Clarithromycin, which is classified as an anti-infective agent. Clarithromycin belongs specifically to the macrolide class of antibiotics, which are utilized for systemic administration to treat various bacterial illnesses. This active substance is semisynthetic, derived from the naturally occurring macrolide, Erythromycin, through a chemical modification designed to enhance its acid stability and improve its bioavailability within the human body. This modification makes Clarithromycin an effective treatment option for susceptible bacterial pathogens.

What is the General Purpose of Clarithromycin?

The fundamental purpose of Clarithromycin is to effectively combat and resolve bacterial infections by eliminating the responsible pathogens. It achieves this by functioning as a protein synthesis inhibitor; the drug enters the bacterial cell and binds to the 50S ribosomal subunit, thereby blocking the machinery required for protein assembly. This mechanism, which is primarily bacteriostatic (stopping growth), prevents the infection from advancing. The macrolide class of drugs is commonly employed to address a broad range of susceptible infections, ensuring the medication limits the spread of infection and assists the immune system in recovery.

In What Forms is Makcin (Clarithromycin) Available?

Clarithromycin is widely formulated for oral intake. The medication is available in several dosage form(s), primarily as both standard, immediate-release tablets and as an oral suspension for liquid dosing. The availability of the liquid oral suspension is a distinguishing feature, making the macrolide accessible for pediatric patients. Furthermore, modified-release tablets are also produced, which are designed to release the active compound slowly over a prolonged period. The availability of multiple oral forms ensures flexible administration and optimizes therapeutic drug levels.

Regulatory References

  1. semisynthetic
  2. macrolide class

What side effects are possible with Makcin (Clarithromycin)?

Possible Side Effects and Safety Information

Makcin (Clarithromycin) is associated with a range of possible side effects, which are officially documented and classified by their frequency and the body system affected. All safety information is strictly derived from regulatory authority documents.

Frequency-Classified Adverse Reactions

  • Common (1 in 100 to 1 in 10 patients): Diarrhea, nausea, vomiting, abdominal pain, altered sense of taste (dysgeusia), headache, insomnia, and abnormal liver function tests.
  • Uncommon (1 in 1,000 to 1 in 100 patients): Vertigo, anxiety, hypersensitivity reactions, leukopenia (low white blood cell count), and gastritis.
  • Not Known (Frequency cannot be estimated): Torsades de Pointes, ventricular tachycardia, hepatic failure, acute pancreatitis, and severe skin reactions like Stevens-Johnson Syndrome (SJS) or Toxic Epidermal Necrolysis (TEN).

Serious Adverse Reactions

Regulatory sources highlight rare but serious adverse reactions, including potentially fatal hepatic failure and severe cardiac events such as QT prolongation leading to Torsades de Pointes.

Safety Restrictions and Limitations

Clarithromycin is contraindicated (must not be used) in patients with a history of cardiac arrhythmias (like QT prolongation), hypokalemia, or pre-existing hepatic failure combined with renal impairment. The drug is generally not recommended during the first trimester of pregnancy.

Dose and Exposure-Related Notes

The risk of Clostridium difficile-associated diarrhea (CDAD) can occur up to two months after stopping the medicine. Furthermore, regulatory agencies have noted a potential for an increased risk of heart problems/death occurring years later in patients with coronary artery disease who received a 14-day course of clarithromycin.

Overdose and Emergency Response

Overdose Map: Overdose and when to seek help — Official Regulatory Information for Makcin (Clarithromycin)

Category Official Regulatory Documentation Statement
Documented overdose presentations: Primarily involves severe gastrointestinal disturbances, including abdominal pain, nausea, vomiting, and diarrhea. Neurological events, such as a confusional state or psychosis, have also been reported in post-marketing experience.
Physiological systems affected (as stated in label): The Gastrointestinal system and the Cardiovascular system (risk of QT prolongation and ventricular arrhythmia, including Torsades de pointes).
Dose-related or exposure-related factors (if applicable): Acute overdose situations typically involve ingestion of a dose level exceeding the standard therapeutic range.
Population-specific overdose notes (if applicable): Overdose symptoms, particularly severe cardiac events and accumulation due to reduced clearance, may be compounded in patients with existing severe kidney impairment.
Emergency-response statements (as written in official documents): Seek emergency medical attention and contact the poison control helpline.
When immediate medical help is required (label-derived phrasing only): Immediately call emergency services if the affected person has collapsed, had a seizure, has trouble breathing, or cannot be awakened.

Overdose Classifications (High-Level)

Category Official Regulatory Documentation Statement
Severity classification (as defined in official documents): Overdose is classified by severe GI symptoms and the potential for life-threatening outcomes such as cardiac arrhythmias.
Regulatory basis (EMA / FDA / etc.): Information is based on official prescribing documents, including the FDA Prescribing Information and the EMA Summary of Product Characteristics.
Overdose-context constraints (as defined in official documents): No specific antidote is known, and standard procedures like hemodialysis or peritoneal dialysis are explicitly stated as not effective for removing the drug.

Resulting Overdose Structure

Official overdose statements:

  • Manifestations include severe GI symptoms (pain, vomiting, diarrhea) and potential psychiatric disturbances.
  • Overdose may lead to severe cardiac arrhythmias, including Torsades de pointes, which is a life-threatening risk.
  • Management is symptomatic and supportive, as no specific antidote is available.
  • Urgent medical attention must be sought immediately if severe critical signs are present.

Connection to the overall overdose profile (3 sentences): The regulatory profile strictly defines Clarithromycin overdose by detailing both common severe gastrointestinal signs and the critical, life-threatening cardiovascular risks. Regulators mandate specific immediate actions, emphasizing the need to call emergency services for critical signs like collapse or seizures. The documentation further guides professional management by stating that treatment is limited to supportive care due to the lack of an available antidote and the ineffectiveness of dialysis.

Therapeutic Uses of Makcin (Clarithromycin)

What Makcin (Clarithromycin) Treats: Main Uses and Benefits

Makcin (Clarithromycin) is used across key therapeutic domains to manage symptoms that interfere with daily functioning. It is commonly applied in clinical settings that involve acute or unstable symptom patterns.

This macrolide antibiotic is commonly used to help address symptom clusters that may become intense or disruptive due to acute bacterial infections of the respiratory tract, such as pneumonia, acute bronchitis, and sinusitis, as well as localized discomfort in the skin and soft tissues. It is also relevant in conditions involving inflammatory or irritative processes, such as those related to Helicobacter pylori infection, and for use in addressing Mycobacterium Avium Complex (MAC) in vulnerable patients.

The medication's application supports the easing of distressing symptoms like persistent cough, fever, pain, and localized inflammatory states, assisting with maintaining functional stability during symptomatic periods. It is also considered relevant as a therapeutic option for patients who cannot use standard treatments due to hypersensitivity.

“This application supports the patient during difficult episodes by easing distress and helps maintain a sense of stability when symptoms are more noticeable.”


Quick Fact: Relief for Acute Symptom Clusters

Clarithromycin is commonly used when acute symptoms of bacterial origin, such as fevers and localized inflammatory pain, cluster together and create noticeable physiological strain, where short-term symptomatic assistance is needed.

Regulatory References

  1. DailyMed Official Label for Clarithromycin

Eligibility and Restrictions for Use

Makcin (Clarithromycin) is subject to strict eligibility rules defined by government regulatory authorities based on patient population and pre-existing conditions. These rules define who is allowed conditional use and who is contraindicated (prohibited) from use.


Eligibility Scope: Official Regulatory Information

Classification Status & Requirements (as stated in the label)
Absolute Contraindications Use is prohibited in patients with macrolide hypersensitivity, known QT prolongation or ventricular arrhythmia, and severe hepatic failure combined with renal impairment.
Age-Related Eligibility Adults and adolescents (12+ years) are eligible. Infants under 6 months are generally not eligible as safety and efficacy are not established. Children under 12 must use the oral suspension form, as tablets are unsuitable.
Organ Function Restriction Eligibility is conditional for severe renal impairment (creatinine clearance < 30 mL/min); the required total daily dose must be reduced by half. Caution is required in patients with non-severe hepatic impairment.
Pregnancy/Lactation Use is not recommended during pregnancy unless alternatives are unavailable and the benefit clearly outweighs the risk. Nursing mothers should discontinue nursing or discard milk during treatment.
Prohibited Co-administration The medicine is contraindicated if concomitantly used with drugs such as Lovastatin, Simvastatin, Pimozide, Ergot alkaloids, Lurasidone, Ticagrelor, Ivabradine, or Ranolazine.

What should I know about interactions with other medicines?

Makcin (Clarithromycin) has a specific interaction profile primarily governed by its capacity to inhibit drug metabolism and transport proteins. Regulatory documents classify this antibiotic as a strong inhibitor of the CYP3A4 enzyme, a metabolic pathway responsible for clearing numerous other medicinal products. This pharmacokinetic action often leads to a substantial increase in the plasma concentration of co-administered drugs.

As a result, certain combinations are strictly contraindicated in official labeling, including Pimozide, Ergot Alkaloids (Ergotamine, Dihydroergotamine), Lovastatin, and Simvastatin, due to the serious risk of increased toxicity or adverse events.

Documented Interaction Patterns

Interaction Type Examples of Affected Substances Constraint or Outcome
Pharmacokinetic Inhibition Carbamazepine, Digoxin, Sildenafil Increased exposure (AUC/Cmax) of the co-administered drug, often requiring monitoring.
Pharmacodynamic Effects Quinidine, Disopyramide, Warfarin Additive effects, such as increased risk of QT prolongation or potentiation of anticoagulant effects.
Timing Rule Extended-Release Tablets only Must be taken with food to prevent a documented 30% reduction in drug exposure.
Population-Specific Note Colchicine Contraindicated in patients with renal or hepatic impairment due to increased toxicity risk.

This structure, defined by strong enzyme and transporter inhibition, establishes the regulatory constraints for safe co-administration.

Mechanism of Action

The Mechanism of Action: Inhibition of Bacterial Protein Synthesis

Clarithromycin exerts its primary pharmacodynamic effect by functioning as an inhibitor that selectively targets the bacterial 50S ribosomal subunit. The molecule non-covalently binds to the 23S ribosomal RNA component of this structure. This precise molecular interaction physically obstructs the peptide exit tunnel , preventing the newly formed polypeptide chains from elongating and releasing. This modification of a core pathway immediately halts the production of proteins essential for bacterial function, growth, and replication, which results in the stasis of bacterial proliferation, a mechanism classified as bacteriostatic.

Constraints on Mechanistic Efficacy

Bacteria can counteract the drug's mechanism, constraining its effectiveness. Resistance mechanisms include the modification of the 23S rRNA, which reduces the drug's binding affinity, and the activation of efflux pumps. These pumps actively transport the Clarithromycin molecule out of the cytoplasm, reducing its concentration at the ribosomal target and leading to a failure to maintain inhibition of protein synthesis.

Dosage and Administration Information

How to Use Makcin (Clarithromycin)

Clarithromycin is administered via the oral route (tablets or suspension) or by intravenous (IV) infusion when oral intake is not feasible. The medicine is available in several official formulations, including 250 mg and 500 mg immediate-release (IR) tablets, a 500 mg extended-release (ER) tablet, and an oral suspension for liquid dosing.


Administration Requirements

Instruction Domain Official Administration Rule
Dosing Frequency IR tablets and the IV form are typically dosed every 12 hours (q12h). ER tablets are dosed once daily (q24h).
Timing with Food IR tablets and suspension may be taken with or without food. ER tablets must be taken with food to ensure correct drug release.
Duration The standard course of treatment typically lasts 7 to 14 days, as specified in regulatory guidelines.
Special Handling Extended-release tablets must be swallowed whole and are not to be crushed, cut, or chewed.

Dosage Adjustments

Official instructions mandate specific adjustments for certain patient populations. For pediatric patients (aged 6 months and older), the dosage is calculated based on body weight, typically 15 mg/kg/day divided into two equal doses. Patients diagnosed with severe renal impairment (Creatinine Clearance < 30 mL/min) require a 50% reduction in the total maximum daily dose. If a dose is missed, it should be taken as soon as remembered, unless the next scheduled dose is nearly due, in which case the missed dose is skipped to prevent double dosing.

Recent Clinical Evidence

Clarithromycin: Recent Clinical Evidence

Clarithromycin is a macrolide antibiotic used to treat a wide variety of bacterial infections. Clinical evidence continues to support its use as an effective agent against susceptible organisms. The primary areas of recent clinical focus include its role in respiratory tract infections, Helicobacter pylori eradication, and non-tuberculous mycobacterial infections.


Respiratory Tract Infections

Clarithromycin remains a treatment option for community-acquired pneumonia (CAP) caused by atypical bacteria, such as Mycoplasma pneumoniae or Chlamydophila pneumoniae. Studies frequently evaluate it as part of combination regimens to ensure coverage against a broad spectrum of pathogens. While resistance rates continue to be monitored globally, evidence suggests its continued utility in areas where local susceptibility patterns are favorable.

H. pylori Eradication

For the treatment of peptic ulcers and gastritis associated with H. pylori infection, Clarithromycin is an essential component of triple or quadruple therapy regimens. Recent clinical guidelines emphasize that the success of Clarithromycin-containing regimens is highly dependent on the local prevalence of Clarithromycin resistance. Treatment recommendations are often tailored based on the patient's prior antibiotic exposure and regional resistance data to maximize eradication rates.

Antimicrobial Research Focus

Beyond standard indications, research explores the anti-inflammatory and immunomodulatory effects of macrolides, including Clarithromycin, in chronic respiratory conditions. However, these applications are generally considered investigational and are not standard therapeutic indications. Research also frequently examines the safety profile of Clarithromycin, particularly concerning its potential to prolong the QT interval on an electrocardiogram, necessitating careful use in patients with pre-existing cardiac risk factors. The overall benefit-risk profile supports its established uses.

Frequently Asked Questions (FAQ)

Common questions about Makcin (Clarithromycin) (FAQ)

Q: Is Makcin a penicillin-based antibiotic?

A: No, Makcin is not a penicillin-based drug. The active ingredient, Clarithromycin, is factually classified as a macrolide antibiotic. This means it belongs to a completely different class of anti-infective agents than penicillin.


Q: Why is a metallic or altered taste a reported side effect of Makcin?

A: Official documents list an altered sense of taste, known as dysgeusia, as a common adverse reaction. Studies referenced in regulatory information indicate that this effect may happen because a portion of the medicine is secreted into the saliva. When the compound reaches the mouth, it can directly stimulate the taste receptors, leading to the metallic or strange sensation.


Q: Is a stomach ache or abdominal discomfort a common side effect of Makcin?

A: Yes, abdominal pain is officially documented as a common adverse reaction associated with Makcin. According to the product information, this type of discomfort may affect between 1 in 100 and 1 in 10 people who use the medicine.


Q: What are the signs of a serious liver problem while taking Makcin?

A: Official regulatory information describes rare but serious liver problems, such as hepatic failure, which have been reported. Signs of potential hepatitis can include loss of appetite, persistent itching, or a tender abdomen. Other symptoms that have been officially reported include yellowing of the skin or eyes (jaundice) or unusually dark urine.


Q: Is feeling dizzy or disoriented a possible side effect of Makcin?

A: The official product information lists vertigo, which is a specific type of dizziness, as an uncommon side effect. This means it may affect between 1 in 1,000 and 1 in 100 patients.


Q: Can Makcin cause difficulty sleeping or nightmares?

A: Difficulty sleeping, known as insomnia, is listed as a common adverse reaction in regulatory documents. While the official classifications cover insomnia, the specific mention of nightmares or other detailed sleep disturbances is not explicitly addressed in the common side effect listings.


Q: Can Makcin cause temporary hearing changes or loss?

A: Official regulatory reports note that temporary hearing changes or loss (ototoxicity) is a reported adverse effect associated with this macrolide class of drugs. Regulatory information notes that this effect has often been reported as reversible following the discontinuation of the medication.


Q: Are there any specific pain medications or over-the-counter drugs that should not be taken with Makcin?

A: Regulatory drug interaction data indicates that Makcin is a strong inhibitor of the CYP3A4 enzyme, which is responsible for processing many other medicines. This action can potentially increase the exposure to certain over-the-counter pain relievers, such as acetaminophen, in the body.


Q: Is it generally considered permissible to drink alcohol while taking Makcin?

A: Official patient information sources generally state that the consumption of alcohol is permissible while taking this medication.


Q: Does Makcin affect the reliability of oral contraceptives or birth control?

A: Official labels document that Clarithromycin can interact with the hormones used in oral contraceptives. This interaction may either increase or decrease the concentration of the hormones in the body, which could potentially lead to breakthrough bleeding or an increased risk of pregnancy.


Q: Can Makcin be used if a person has a history of Myasthenia Gravis?

A: Regulatory documents state that caution is required regarding the use of Makcin in the presence of Myasthenia Gravis. Official warnings state that this medication may potentially worsen the symptoms associated with this condition.


Q: Are there any specific herbal supplements known to interact with Makcin?

A: Official guidance frequently notes that there is often insufficient information available to confirm the safety or lack of interaction between Makcin and many herbal or complementary remedies. Official product information suggests that compatibility with supplements should be confirmed.


Q: Is there a distinction between the effects of the standard tablet and the extended-release tablet of Makcin?

A: Yes, the two forms differ in their officially approved uses. Regulatory documents indicate that the extended-release tablet is approved for a more limited set of indications (specific uses) compared to the standard immediate-release tablet form.


Q: What information is available about Makcin compared to Azithromycin (another macrolide)?

A: Regulatory documents establish differences in how these two macrolide antibiotics are used. Regulatory information notes that the approved regimen for Clarithromycin is typically twice daily, while Azithromycin regimens are often once daily. Additionally, only Clarithromycin is specified in the official labeling as a component for H. pylori eradication treatment regimens.

How should Makcin (Clarithromycin) be stored and disposed of?

How to Store and Dispose of Makcin (Clarithromycin)

The storage of Clarithromycin is strictly defined by regulatory labeling to ensure product stability and safety.

Clarithromycin tablets must be stored at room temperature, typically below 25 C or 30 C, and must be protected from moisture and light.


Form-Specific Storage and Disposal Rules

The oral suspension (liquid form) requires specific handling: once mixed, the product must not be refrigerated or frozen and must be discarded after 14 days.

All forms of the medication must be stored out of the sight and reach of children.

Disposal instructions mandate that unused or expired Clarithromycin must not be thrown away with household waste or wastewater. The product must be disposed of in accordance with local regulations, often by returning it to a pharmacist for proper handling.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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